Mintern Justine D, Macri Christophe, Chin Wei Jin, Panozza Scott E, Segura Elodie, Patterson Natalie L, Zeller Peter, Bourges Dorothee, Bedoui Sammy, McMillan Paul J, Idris Adi, Nowell Cameron J, Brown Andrew, Radford Kristen J, Johnston Angus Pr, Villadangos Jose A
a Walter and Eliza Hall Institute ; Parkville , VIC Australia.
Autophagy. 2015;11(6):906-17. doi: 10.1080/15548627.2015.1045178.
Antigen-presenting cells survey their environment and present captured antigens bound to major histocompatibility complex (MHC) molecules. Formation of MHC-antigen complexes occurs in specialized compartments where multiple protein trafficking routes, still incompletely understood, converge. Autophagy is a route that enables the presentation of cytosolic antigen by MHC class II molecules. Some reports also implicate autophagy in the presentation of extracellular, endocytosed antigen by MHC class I molecules, a pathway termed "cross-presentation." The role of autophagy in cross-presentation is controversial. This may be due to studies using different types of antigen presenting cells for which the use of autophagy is not well defined. Here we report that active use of autophagy is evident only in DC subtypes specialized in cross-presentation. However, the contribution of autophagy to cross-presentation varied depending on the form of antigen: it was negligible in the case of cell-associated antigen or antigen delivered via receptor-mediated endocytosis, but more prominent when the antigen was a soluble protein. These findings highlight the differential use of autophagy and its machinery by primary cells equipped with specific immune function, and prompt careful reassessment of the participation of this endocytic pathway in antigen cross-presentation.
抗原呈递细胞监测其周围环境,并呈递与主要组织相容性复合体(MHC)分子结合的捕获抗原。MHC-抗原复合物的形成发生在特定的区室中,多条蛋白质运输途径在此汇聚,目前仍未完全了解这些途径。自噬是一种使MHC II类分子呈递胞质抗原的途径。一些报告还表明自噬参与了MHC I类分子对细胞外、内吞抗原的呈递,这一途径被称为“交叉呈递”。自噬在交叉呈递中的作用存在争议。这可能是由于使用了不同类型的抗原呈递细胞进行研究,而对于这些细胞自噬的使用定义并不明确。在此我们报告,自噬的积极作用仅在专门进行交叉呈递的树突状细胞亚型中明显。然而,自噬对交叉呈递的贡献因抗原形式而异:在细胞相关抗原或通过受体介导的内吞作用递送的抗原情况下可忽略不计,但当抗原为可溶性蛋白时则更为显著。这些发现突出了具有特定免疫功能的原代细胞对自噬及其机制的不同利用情况,并促使人们仔细重新评估这一内吞途径在抗原交叉呈递中的参与情况。